All diseases

OMIM ID
171400
OMIM term:
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA; MEN2A
Alternative terms:
PHEOCHROMOCYTOMA AND AMYLOID-PRODUCING MEDULLARY THYROID CARCINOMA
PTC SYNDROME
SIPPLE SYNDROME THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
(∗) Location:
10q11.21  
(†) Associated OMIM genes:
RET  
(‡) Associated MGI genes:

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